Robert William Davies
Robert William Davies
Department of Statistics, University of Oxford
Potvrđena adresa e-pošte na - Početna stranica
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333-338, 2011
Meta-analysis identifies six new susceptibility loci for atrial fibrillation
PT Ellinor, KL Lunetta, CM Albert, NL Glazer, MD Ritchie, AV Smith, ...
Nature genetics 44 (6), 670-675, 2012
Low copy number of the salivary amylase gene predisposes to obesity
M Falchi, JS El-Sayed Moustafa, P Takousis, F Pesce, A Bonnefond, ...
Nature genetics 46 (5), 492-497, 2014
Genomic analyses from non-invasive prenatal testing reveal genetic associations, patterns of viral infections, and Chinese population history
S Liu, S Huang, F Chen, L Zhao, Y Yuan, SS Francis, L Fang, Z Li, L Lin, ...
Cell 175 (2), 347-359. e14, 2018
Sequencing of human genomes with nanopore technology
R Bowden, RW Davies, A Heger, AT Pagnamenta, M de Cesare, ...
Nature communications 10 (1), 1869, 2019
Rapid genotype imputation from sequence without reference panels
RW Davies, J Flint, S Myers, R Mott
Nature genetics 48 (8), 965-969, 2016
Rare copy number variants contribute to congenital left-sided heart disease
MP Hitz, LP Lemieux-Perreault, C Marshall, Y Feroz-Zada, R Davies, ...
Public Library of Science 8 (9), e1002903, 2012
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex
RW Davies, GA Wells, AFR Stewart, J Erdmann, SH Shah, JF Ferguson, ...
Circulation: Cardiovascular Genetics 5 (2), 217-225, 2012
Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing
J Nicod, RW Davies, N Cai, C Hassett, L Goodstadt, C Cosgrove, BK Yee, ...
Nature genetics 48 (8), 912-918, 2016
Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies
RW Davies, S Dandona, AFR Stewart, L Chen, SG Ellis, WH Wilson Tang, ...
Circulation: Cardiovascular Genetics 3 (5), 468-474, 2010
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11. 2 deletion syndrome
RW Davies, AM Fiksinski, EJ Breetvelt, NM Williams, SR Hooper, ...
Nature medicine 26 (12), 1912-1918, 2020
A high-resolution map of non-crossover events reveals impacts of genetic diversity on mammalian meiotic recombination
R Li, E Bitoun, N Altemose, RW Davies, B Davies, SR Myers
Nature communications 10 (1), 3900, 2019
Haplotype tagging reveals parallel formation of hybrid races in two butterfly species
JI Meier, PA Salazar, M Kučka, RW Davies, A Dréau, I Aldás, ...
Proceedings of the National Academy of Sciences 118 (25), e2015005118, 2021
Inflammation and coronary artery disease: insights from genetic studies
R McPherson, RW Davies
Canadian Journal of Cardiology 28 (6), 662-666, 2012
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy
JD Roberts, NP Murphy, RM Hamilton, ER Lubbers, CA James, CF Kline, ...
The Journal of Clinical Investigation 129 (8), 3171-3184, 2019
Rapid genotype imputation from sequence with reference panels
RW Davies, M Kucka, D Su, S Shi, M Flanagan, CM Cunniff, YF Chan, ...
Nature genetics 53 (7), 1104-1111, 2021
Torsades de pointes during complete atrioventricular block: Genetic factors and electrocardiogram correlates
RN Subbiah, MH Gollob, LJ Gula, RW Davies, P Leong-Sit, AC Skanes, ...
Canadian Journal of Cardiology 26 (4), 208-212, 2010
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders
L D’Abate, S Walker, RKC Yuen, K Tammimies, JA Buchanan, RW Davies, ...
Nature communications 10 (1), 5519, 2019
Adiposity significantly modifies genetic risk for dyslipidemia [S]
CB Cole, M Nikpay, P Lau, AFR Stewart, RW Davies, GA Wells, R Dent, ...
Journal of lipid research 55 (11), 2416-2422, 2014
Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation
JD Roberts, RW Davies, SA Lubitz, IL Thibodeau, PB Nery, DH Birnie, ...
Europace 12 (8), 1078-1083, 2010
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